COVID-19 and metabolic comorbidities: An update on emerging evidences for optimal therapies

被引:11
作者
Hua, Shuang [1 ,2 ]
Yang, Yong [1 ,2 ]
Zou, Danqi [1 ,2 ]
Li, Jufei [1 ,2 ]
Yan, Kaixuan [1 ,2 ]
Xu, Ying [3 ]
Jiang, Xue [1 ,2 ]
Rong, Xianglu [1 ,2 ]
Ye, Dewei [1 ,2 ]
机构
[1] Minist Educ, Key Lab Glucolipid Metab Dis, Guangzhou, Peoples R China
[2] Guangdong Pharmaceut Univ, Guangdong Metab Dis Res Ctr Integrated Chinese &, Guangzhou, Peoples R China
[3] Guangdong Pharmaceut Univ, Sch Clin Med, Affiliated Hosp 1, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Diabetes; Metabolic comorbidities; COVID-19; Hypertension; ANGIOTENSIN-CONVERTING ENZYME; NECROSIS-FACTOR-ALPHA; INSULIN-RESISTANCE; SARS-COV-2; ACE2; CORONAVIRUS; MORTALITY; INFECTION; ENTRY; PATHOGENESIS;
D O I
10.1016/j.biopha.2021.111685
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Type 2 diabetes mellitus, obesity, hypertension, and other associated metabolic complications have been demonstrated as a crucial contributor to the enhanced morbidity and mortality of patients with coronavirus disease 2019 (COVID-19). Data on the interplay between metabolic comorbidities and the outcomes in patients with COVID-19 have been emerging and rapidly increasing. This implies a mechanistic link between metabolic diseases and COVID-19 resulting in the exacerbation of the condition. Nonetheless, new evidences are emerging to support insulin-mediated aggressive glucose-lowering treatment as a possible trigger of high mortality rate in diabetic COVID-19 patients, putting the clinician in a confounding and difficult dilemma for the treatment of COVID-19 patients with metabolic comorbidities. Thus, this review discusses the pathophysiological link among severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), angiotensin-converting enzyme 2 (ACE2), metabolic complications, and severe inflammation in COVID-19 development, especially in those with multiorgan injuries. We discuss the influence of several routinely used drugs in COVID-19 patients, including antiinflammatory and anti-coagulant drugs, antidiabetic drugs, renin-angiotensin-aldosterone system inhibitors. Especially, we provide a balanced overview on the clinical application of glucose-lowering drugs (insulin and metformin), angiotensin-converting-enzyme inhibitors, and angiotensin receptor blockers. Although there is insufficient evidence from clinical or basic research to comprehensively reveal the mechanistic link between adverse outcomes in COVID-19 and metabolic comorbidities, it is hoped that the update in the current review may help to better outline the optimal strategies for clinical management of COVID-19 patients with metabolic comorbidities.
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页数:8
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